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3. Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27. Trump D; Dixon PH; Mumm S; Wooding C; Davies KE; Schlessinger D; Whyte MP; Thakker RV J Med Genet; 1998 Nov; 35(11):905-9. PubMed ID: 9832036 [TBL] [Abstract][Full Text] [Related]
4. [Analysis of the polymorphism of primary myopathies with recessive X-linked inheritance]. Grinio LP Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1621-4. PubMed ID: 7324662 [TBL] [Abstract][Full Text] [Related]
5. Primary familial hypoparathyroidism with an autosomal dominant mode of inheritance. De Campo C; Piscopello L; Noacco C; Da Col P; Englaro GC; Benedetti A J Endocrinol Invest; 1988 Feb; 11(2):91-6. PubMed ID: 3361084 [TBL] [Abstract][Full Text] [Related]
6. A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism. Pillar N; Pleniceanu O; Fang M; Ziv L; Lahav E; Botchan S; Cheng L; Dekel B; Shomron N Hum Genet; 2017 Jul; 136(7):835-845. PubMed ID: 28444561 [TBL] [Abstract][Full Text] [Related]
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19. A case of chromosome 22q11 deletion syndrome diagnosed in a 32-year-old man with hypoparathyroidism. Maalouf NM; Sakhaee K; Odvina CV J Clin Endocrinol Metab; 2004 Oct; 89(10):4817-20. PubMed ID: 15472168 [TBL] [Abstract][Full Text] [Related]
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